Evidence map›Paper›PMID 42738908›Full record

ReviewCells2026

Cellular Senescence in Blood Cells: A Link Between Metabolic Syndrome, Inflammaging and Cardiometabolic Disease.

Katerina Gioti, Maria Trapali, Irene Belouka, Dimitrios Chaniotis, Apostolos Beloukas

Abstract readReview
In one paragraph

Review in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Katerina GiotiDepartment of Biomedical Sciences, School of Health Sciences, University of West Attica, 12243 Athens, Greece.ORCID 0000-0002-2698-9772
Maria TrapaliDepartment of Biomedical Sciences, School of Health Sciences, University of West Attica, 12243 Athens, Greece.ORCID 0000-0001-8785-7522
Irene BeloukaDepartment of Biomedical Sciences, School of Health Sciences, University of West Attica, 12243 Athens, Greece.
Dimitrios ChaniotisDepartment of Biomedical Sciences, School of Health Sciences, University of West Attica, 12243 Athens, Greece.ORCID 0000-0003-2313-1305
Apostolos BeloukasDepartment of Biomedical Sciences, School of Health Sciences, University of West Attica, 12243 Athens, Greece.ORCID 0000-0001-5639-0528

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic syndrome (MetS) is a complex metabolic disorder characterized by central obesity, insulin resistance, dyslipidemia, hypertension, and chronic low-grade inflammation, all of which contribute to an increased risk of type 2 diabetes mellitus, cardiovascular disease, and premature mortality. Emerging evidence suggests that cellular senescence plays a central role in the pathophysiology of MetS by linking metabolic stress to chronic inflammation, immune dysfunction, as well as cell and tissue damage. Although senescence has traditionally been studied in tissue-resident cells, growing attention has focused on the role of blood-cell senescence in the initiation and progression of metabolic disease. This review summarizes current knowledge regarding the molecular and cellular mechanisms driving senescence in hematopoietic stem cells and circulating blood-cells (BCs) and how these mechanisms affect specific blood-cell populations leading to altered immune function, impaired tissue homeostasis, and persistent inflammatory activation. The link between clonal hematopoiesis to immunosenescence and cardiometabolic disease is also highlighted, providing additional insight into the complex interactions between hematopoietic aging and metabolic dysfunction.

Indexed as

Blood CellsCardiovascular DiseasesCellular SenescenceInflammationMetabolic SyndromeAnimalsHumansblood cellscellular senescenceclonal hematopoiesisimmunosenescenceinflammagingmetabolic inflammationmetabolic syndromemitochondrial dysfunctionoxidative stresssenescence-associated secretory phenotype (SASP)

Identifiers

PMID42738908
PMCPMC13565007

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.